Involvement of MdWRKY40 in the defense of mycorrhizal apple against fusarium solani

Background Apple (Malus domestica Borkh.) is an important economic crop. The pathological effects of Fusarium solani, a species complex of soilborne pathogens, on the root systems of apple plants was unknown. It was unclear how mycorrhizal apple seedlings resist infection by F. solani. The transcriptional profiles of mycorrhizal and non-mycorrhizal plants infected by F. solani were compared using RNA-Seq. Results Infection with F. solani significantly reduced the dry weight of apple roots, and the roots of mycorrhizal apple plants were less damaged when the plants were infected with F. solani. They also had enhanced activity of antioxidant enzymes and a reduction in the oxidation of membrane lipids. A total of 1839 differentially expressed genes (DEGs) were obtained after mycorrhizal and non-mycorrhizal apple plants were infected with F. solani. A gene ontogeny (GO) analysis showed that most of the DEGs were involved in the binding of ADP and calcium ions. In addition, based on a MapMan analysis, a large number of DEGs were found to be involved in the response of mycorrhizal plants to stress. Among them, the overexpressed transcription factor MdWRKY40 significantly improved the resistance of the apple ‘Orin’ callus to F. solani and the expression of the resistance gene MdGLU by binding the promoter of MdGLU. Conclusion This paper outlines how the inoculation of apple seedlings roots by arbuscular mycorrhizal fungi responded to infection with F. solani at the transcriptional level. In addition, MdWRKY40 played an important role in the resistance of mycorrhizal apple seedlings to infection with F. solani. Supplementary Information The online version contains supplementary material available at 10.1186/s12870-022-03753-z.

on apple roots [10,14]. Those series of physiologic and biochemical reactions can lead to severe root tip necrosis and decay until plant death occurs several days or weeks after F. solani infection [15]. Therefore, it is urgent to find an effective method to enhance the resistance of apple rootstocks to F. solani.
Arbuscular mycorrhizal fungi (AMF) can infect more than two-thirds of terrestrial plants to form efficient symbiotic relationships on the roots [16]. There is an interaction among AMF, pathogens, and plants [17]. AMF can not only enhance the resistance of the host to environmental stress, such as drought and salt stress, by improving the efficiency of utilization of plant nutrients [18,19], but also have a significant effect on the induction of plant resistance to soilborne diseases and improve the growth of host plants [20,21]. Previous studies have shown that AMF effectively provide biological control against soilborne pathogens, such as F. oxysporum, Sclerotium cepivorum and Pythium aphanidermatum [22]. AMF prevent and control soilborne diseases by challenging the growth sites of pathogens in the root systems of host plants and produce wide networks of extraradical mycelia [23,24]. The AMF-plant symbiotic relationship results in enhanced plant growth, which may be stimulated through several activities, including regulation of the secondary metabolic pathway of the roots of host plants, the increased synthesis and secretion of terpenes and phenolic compounds, promotion of the synthesis of antimicrobial substances, and improvements in the plant defense system [25,26]. An important number of genes related to hormone signalling are involved in the enhanced resistance or tolerance of mycorrhizal plants to infection by F. virguliforme [27]. The systems of mycorrhizal plants play an active role in the disease resistance process, and plants with mycorrhizae are generally more resistant to soilborne pathogens than plants that lack them [28,29]. The induction of defense responses in mycorrhizal plants was much higher and more quickly than that in non-mycorrhizal plants when infected by pathogens [29]. However, it is unclear how the physiological and molecular responses of mycorrhizal and nonmycorrhizal prevent the infection of apple seedlings with F. solani.
In this study, the apple stock M9T337 was used as the experimental material to explore the defense mechanism of mycorrhizal apple seedlings. Several experimental evaluations of the pre-inoculation of AMF were conducted to help improve the resistance of apple root systems to F. solani. We hypothesized that the presence of symbiotic apple root systems enhances resistance to F. solani. Therefore, the molecular mechanism of the AMF-apple interaction in response to the infection was analyzed by transcriptome. This study provides a basis for understanding the molecular mechanism of mycorrhizal apple defence against infection by F. solani.

Physiological properties of mycorrhizal apple roots
The plants were harvested 10 days after infection with F. solani. No colonization was detected in the non-inoculated AMF seedlings, including NM (non-mycorrhizal plants that had not been inoculated with F. solani) and NM-F (non-mycorrhizal plants inoculated with F. solani) treatments. In the AMF inoculated plants, AMF and plant roots had established a symbiotic relationship with a colonization rate of 76% in the AM treatment (mycorrhizal plants that had not been inoculated with F. solani), but after infection with F. solani, the colonization rate was 49% in AM-F treatment (mycorrhizal plants inoculated with F. solani). Infection with F. solani significantly reduced the dry weight of plants, and the presence of AMF in plants that had been inoculated with F. solani significantly reduced the damage of F. solani to the plants. The activity of superoxide dismutase (SOD) of the AM was significantly higher than that of the NM treatment, while the activities of other antioxidant enzymes did not differ significantly from the NM treatment. After 5 days of infection with F. solani, the SOD and peroxidase (POD) activities of the AM-F treatment increased by 12.5 and 56.4%, respectively, compared with the NM-F treatment, while there was no significant difference in the activity of catalase (CAT) (Fig. 2A). The contents of malondialdehyde (MDA), hydrogen peroxide (H 2 O 2 ), and superoxide (O 2 · − ) in the AMF symbiotic plants were 19.8, 26.1, and 54.2% lower than those in the non-mycorrhizal plants, respectively (Fig. 2B). We also observed a similar trend in the contents of proline (PRO), soluble protein, and soluble sugar (SOG) in the treated plant roots that correlated with the activities of SOD and POD (Fig. 2C).

DEG screening
To investigate changes in the level of transcription of apple rootstock M9T337 root after inoculation with AMF and F. solani, different treatments were assessed. The differentially expressed genes (DEGs) from the four treatments that were enriched and depleted are shown in Fig. 3. A total of 809 DEGs were identified in the AM-F vs. AM treatment, and 996 DEGs were identified in the NM-F vs. NM treatment. A total of 1839 DEGs, the highest number of differential genes, were identified for subsequent differential gene analysis in the AM-F vs. NM-F treatment. The PCA analysis identified a significant separation between the AM-F and NM-F (Fig. S3).
This experiment demonstrated that there are different expression of multiple members of different TF families, including the WRKY, AP2-ERF, bHLH, NAC, MYB, HB, C2H2, and bHLH families (Fig. 4B). There is a class of proteins designated ethylene response factors in TFs that are closely related to this signaling pathway, and the differential expression analysis also verified the relevant data. A large number of genes (MD15G1221100, MD07G1248600, MD05G1311400, MD04G1058200, MD09G1114800, MD15G1055200, MD02G1096500, MD05G1080900, MD10G1094700) were up regulated in ERF family members by infection with F. solani after 5 days. Interestingly, the most representative class of TFs were the positive regulatory induction of the WRKY family genes in mycorrhizal plants. MdWRKY40, MdWRKY41, MdWRKY53, MdWRKY50, MdWRKY24, MdWRKY76, MdWRKY28, and MdWRKY6 were significantly up regulated in the AM-F vs. NM-F treatment.

MapMan analysis
To provide a more comprehensive understanding of the DEGs in interactions of plants and pathogens, we performed a MapMan visual analysis in biotic stress, secondary metabolism (Fig. 5). The genes that encode TIR-NBS-LRR and NB-ARC were up regulated by F. solani infected. A large number of genes that are related to hormone signaling, including auxin, brassinolide, abscisic acid, ethylene, jasmonic acid, and salicylic acid; pathogenesis-related proteins, such as PR1 and PR5; and transcription factors, such as WRKY, MYB, ERF and DOF, were enriched (Fig. 5A). MdMPK1 and MdMPK18 were up-regulated in the mitogen-activated protein kinase (MAPK) signal pathway.
The biosynthesis of lignin and lignans, flavonoids, phenylpropanoids, and glucosinolates provided the primary secondary metabolic pathways (Fig. 5B). Glucosinolate biosynthesis is thought to produce a chemical barrier against pathogen infection. Nine genes are involved in its for the biosynthetic process, of which only two genes were significantly down regulated. In addition, MD15G1079200, acyl transferase 9 (MD09G1169600), 4-coumarate--CoA ligase-like 5 (MD07G1073800), cinnamoyl-CoA reductase 1 (MD09G1224200), and probable cinnamyl alcohol dehydrogenase 6 (MD15G1008100) in the phenylpropanoid synthesis pathway were significantly upregulated. The solely salicylic acid 3-hydroxylase (MD03G1140400) and hydroquinone glucosyltransferase (MD01G1077200) were up regulated in flavonoid synthesis pathway, seven DEGs were down regulated. Interestingly, DEGs were all up regulated in both the carotenoids and the simple phenolic synthesis pathways.

Quantitative reverse transcription-PCR (qRT-PCR) validation
Based on the sequencing data from our transcriptional group to validate the RNA-Seq results, 16 upregulated genes and six downregulated genes were verified with qRT-PCR (Fig. 6A). The candidate genes were selected to examine their participation in the process of interaction between plants and pathogens, including a pathogen recognition receptor, signal transduction, transcription factor, and the genes involved in the synthesis of secondary metabolites (Fig. 5). These genes could play an important role in the mycorrhizal plant in response to biological stress reactions by infection with F. solani. As shown in Fig. 6B, the trend toward the levels of expression in RNA-Seq and qRT-PCR data was similar, which highlights the reliability of RNA-Seq.

Overexpression of MdWRKY40 improves the resistance of 'Orin' to F. solani
We found the highest relative level of expression of MdWRKY40 (MD15G1039500) in qRT-PCR validation (Table S3). The open reading frame (ORF) of MdWRKY40 was 912 bp, encoding a 303 amino acid, with one conserved WRKY domain and a zinc-finger motif (Fig. S5). To validate the resistance of MdWRKY40 to F. solani, MdWRKY40 was chosen to transform the apple callus. Compared with the wild-type (WT) and OE-MdWRKY40 'Orin' callus that had been infected with F. solani after 4 days, the diameter of fungal spots in the OE-MdWRKY40 was significantly lower than that in the WT, and the diameter of plaque extension in calli was decreased by 56.4% (Fig. 7B,C). To study whether MdWRKY40 regulates the expression of resistance genes, the relative levels of expression of MdPR1, MdPR4, MdPR5, MdPR8, MdECHT, and MdGLU in callus following infection with F. solani were measured by qRT-PCR (Fig. 7D). The levels of expression of MdGLU in OE-MdWRKY40 were significantly higher than the levels in wild type (WT) in all the resistance genes tested (P < 0.01). This suggests that MdWRKY40 could improve the resistance of callus to F. solani by regulating the expression of MdGLU.

MdWRKY40 bound to the MdGLU promoter
Previous studies showed that the WRKY transcription factors usually target W-box motifs to activate or inhibit the level of expression of downstream genes [30]. The promoters of MdGLU contain three W-boxes (Fig. S5). A yeast one-hybrid test was used to determine whether MdWRKY40 combined with the MdGLU promoter. On the media that lacked Trp and His, the optimal concentration to inhibit the expression of HIS3 in the pHIS2 vector was 120 mm 3-amino-1,2,4-triazole (3-AT) for proMdECHT-pHIS2 (Fig. 8B). In the Y1H assays, MdWRKY40 interacted with the promoters of MdGLU. When WRKY40 was divided into two fragments (N-terminus and C-terminus), we found that the C-terminus that contains the WRKY domain bound to the MdGLU promoter ( Fig. 8C). An electrophoretic mobility shift assay (EMSA) confirmed that MdWRKY40 could bind to the second W-box in the MdGLU promoter but not to the other three W-boxes (Fig. 8D, Fig. S6). As the concentration of the cold probe increased, the binding weakened, and the addition of the mutant cold probe did not affect the binding. To determine how MdWRKY40 regulates the level of proMdGLU activity, luciferase (LUC) reporter assays were performed. MdWRKY40 stimulated the expression of the LUC gene driven by the promoter of MdGLU (Fig. 8E). These results indicated that MdWRKY40 activated proMdGLU.

Mycorrhizal symbiosis improved the resistance of apple seedling to F. solani
The symbiosis of AMF with plant roots is often mutually beneficial. After establishing a symbiotic system with the host plant roots, the AMF will promote root development and increase the root biomass [31]. A large amount of research has shown that mycorrhizal plants tend to have more developed roots to absorb essential moisture and nutrients for the host plants under adverse conditions [19,21]. The symbiosis of AMF not only enhances the absorption of soil nutrients by host plant roots but also creates the mycorrhizal pathway for nutrient uptake by the AM fungal mycelia, and plays an important role in the management of abiotic and biotic stress by the plant [32]. In this study, the root length of M9T337 was significantly reduced after infection by F. solani. The pre-inoculation of AMF promoted root growth, indicating that after AMF colonized the plant root system, the soilborne pathogens competed with their ecological niche and reduced their rate of invasion on the root epidermis ( Fig. 1). Simultaneously, after the formation of mycorrhizal plants, a developed mycorrhizal network formed a frontal physical barrier with the root system, could help the plants to more effectively resist the harm caused by pathogens to plants [33,34]. AMF inoculated reduce mortalities root changing activities of lignification and increase isozymes against F. oxysporum infection. After AMF colonized the plant root system, the lignification degree and the resistance related enzymes activity of mycorrhizal plants roots were increased to resist the infection of F. oxysporum, thus reducing the incidence rate [35].
F. solani, as a plant pathogenic fungus, frequently cause a large amount of necrosis of the roots, resulting in a decline in their photosynthetic ability and other pathological changes [10]. When pathogenic fungi infect plants, the resistance of mycorrhizal plant is often induced during the early stages of infection to reduce the damage of pathogens to plants [28]. Studies have shown that Funneliformis mosseae, Rhizophagus irregularis, and other AMF have been used to varying degrees to reduce plant diseases caused by pathogenic fungi [36,37]. Consistent with previous studies, AMF significantly improved the resistance of plants by improving the activities of plant defense enzymes, reducing the oxidation of membrane lipids, and enhancing the plant antioxidant prevention system (Fig. 2). These findings suggest that AMF symbiosis reduced the degree of membrane oxidation and improved the antioxidant activities and permeable regulatory material content to protect the apple root system.

Mycorrhizal plants respond to F. solani infection
The plant-AMF-pathogen interaction is a complex network system that involves multiple gene expression and complex regulation [34,38]. After the pathogens invade plants, the plant will increase the expression of resistance genes and promote the transmission of signal substances and plant metabolism to respond quickly to pathogenic infections [39]. Transcriptome data provide the expression of information and the level of expression for genes that are commonly used to identify the differential stresses of functional plants to biological and non-biological factors [40,41]. To further understand the biological function of the DEGs, we performed GO Pathway significant enrichment and MapMan visualization analyses to determine key differential genes for the main physiological and biochemical metabolic pathways and signal transduction pathways. There were significant morphological differences between the AM and NM roots after pre-inoculation with AMF (Fig. 1). In addition, there were significant differences between gene expression and the DEGs between the AM and NM after infection with F. solani (Fig. 3). In the GO enrichment analysis, more DEGs were concentrated in molecular function, with the most upregulated genes found in the ADP binding (GO:0043531) and calcium ion binding (GO:0005509) pathways (Fig. 4A). The shock of calcium ion concentration in the cytoplasm of root epidermal cells is a central signal factor for plant symbiosis with AMF. The calciumdependent protein kinase activates downstream calcium/ calcium-dependent protein kinases to induce the expression of genes related to symbioses [42]. In the presence of pathogens, AMF constantly competes with pathogens to invade sites on the plant root system, and thus, increases the expression of calmodulin protein genes, such as MdCML37 and MdCML38 (Fig. 5). The plant cells sense that calmodulin was activated in a relative stress response to protect the cells from a high infiltration environment [43,44].
During the process of the interactions of plants with pathogens, a series of defense mechanisms were formed, and the metabolic routes described above were closely related to the defense responses of plants. The related genes of apple-AMF symbionts were analyzed using a MapMan analysis to more comprehensively show the changes of genes in related pathways between mycorrhizal and non-mycorrhizal plants by infection with F. solani. Cells respond to stress through signaling transduction and the intracellular regulation of plant phy siological and biochemical reactions, while the MAPK signaling transduction pathway is in the center of cell signal transduction system [45]. Huang et al. [46] found that the inoculation of AMF resulted in a significant upregulation of MdMAPK, along with the functional response of MdMAPKs to plant hormone signaling and stress responses under drought stress. Plant hormone signal transduction played an important role in the interactions of mycorrhizae to protect the plants against pathogens [47]. In this study, we identified a significant upregulation of hormone signaling genes and numerous PR genes. The MAPK signaling pathway and the plant hormone signal transduction were essential for the resistance of mycorrhizal plants to pathogens, but the deeper molecular mechanisms still merit further research.

TFs respond to mycorrhizal plant resistance to F. solani
TFs play an important role in the process of the plant response to the environment [48,49]. Extensive studies have shown that the families of transcription factors, such as WRKY, AP2, NAC, MYB, and GRAS, are involved in the regulation of expression of defense-related genes (Fig. 4B). In this study, a large number of AP2, WRKY and MYB transcription factor family genes were involved in the response of mycorrhizal plants against infection with F. solani. Only one gene with diminished expression of the WRKY transcription factor was detected in the transcription, and the others increased significantly. The log2 Fold Change of MdWRKY76, MdWRKY53, and MdWRKY40 was more than 2.5-fold (Fig. 6). The results of qRT-PCR were consistent with the RNA-Seq data, and MdWRKY40 was expressed up to 3.69-fold (Table S3).
The overexpression of VvWRKY18 enhances the resistance of Arabidopsis thaliana to Botrytis cinerea through activation of the STILBENE SYNTHASE (STS) genes [50]. The overexpression of HbWRKY40 induced resistance to Colletotrichum gloeosporioides in tobacco [51]. An evolutionary tree analysis found that MdWRKY40 is a member of WRKY IIa (Fig. S7). We hypothesize that MdWRKY40 played a positive role when mycorrhizal plant roots were infected by F. solani. Therefore, the functional validation of MdWRKY40 was performed (Fig. 7). And through its overexpression in "Orin" calli that the overexpression of MdWRKY40 enhanced the resistance to F. solani and improved the level of transcription of MdGLU. YIH, EMSA and LUC report analyses identified the binding of MdWRKY40 to the MdGLU promoter, which indicates that it is, involved in the resistance of apple to infection by F. solani (Fig. 8).

Conclusions
The apple seedlings with AMF significantly reduced the deleterious effects of F. solani to the root system, improved the antioxidant enzyme activities, and reduced  the degree of membrane lipid oxidation. Most of the DEGs involved in plant pathogen interaction, glycolysis/ gluconeogenesis, and hormone signal transduction pathway were identified through GO analyses. The mycorrhizal and non-mycorrhizal apple plants were subjected to oxidative stress after inoculation with F. solani. However, compared with non-mycorrhizal plants, an enormous number of resistance genes were involved in the stress response process to reduce the amount of oxidative damage. MdWRKY40 improved its expression by binding with the MdGLU promoter to participate in mycorrhizal apple seedlings against the infection of F. solani.

Plant growth and plant infection
Apple stock M9T337 was grown in an illuminated greenhouse at 20-30 °C (daytime) and 0-15 °C (night) with a relative humidity of 55-65%. The apple stock M9T337 was obtained from Shandong Horticultural Techniques Services Co., Ltd., Tai'an, Shandong, China. The 'Orin' apple callus was provided by Prof. Xue-sen Chen of the State Key Laboratory of Crop Biology (Tai'an, China). The appropriate permission was obtained for the plant collection and it's use was executed in accordance with relevant guidelines. 'Orin' apple calli (Malus domestica cv. 'Orin') were cultured in subculture medium that contained MS, 2.5 mg·L − 1 2,4-D, and 0.5 mg·L − 1 6-indole-3-butyric acid at room temperature in the dark, and the subculture medium was renewed every 15 days for genetic transformation. F. solani (MG836251.1) was isolated from the roots of a replanted apple tree (Fig. S1) [52]. The hyphae of F. solani were inoculated in sterilized Potato Dextrose Broth (PDB) media and cultured in a shaker at 28 °C for one week. The hyphae were filtered with sterile gauze, and the number of plates was counted. The spores were adjusted to 10 5 ·mL − 1 with sterile water. Arbuscular mycorrhizal fungi used in this study was Paraglomus sp. SW1 (CGMCCNO. 20,744), which was provided by Shandong Agricultural University (Tai'an, China). The inoculant was a mixture of vermiculite, spores (spore density 28·g − 1 ), hyphae and colonized root segments. The systems of mycorrhizal plant roots were grown for 4 weeks using Paraglomus sp. SW1. We established four treatments: (1) NM: non-mycorrhizal plants that had not been inoculated with F. solani; (2) AM: mycorrhizal plants that had not been inoculated with F. solani; (3) NM-F: non-mycorrhizal plants inoculated with F. solani; and (4) AM-F: mycorrhizal plants inoculated with F. solani. After the apple stock M9T337 plantlets grew for 4 weeks with 1% AMF inoculum, 50 mL of a solution of F. solani spores was used to treat them. After 5 days, the apple roots were collected for transcriptome sequencing, qRT-PCR verification, and an analysis of the enzymes involved in resistance. The apple seedlings were randomly collected after 10 days post-infection to determine the apple biomass, root morphology and mycorrhizal colonization rate.

Rate of mycorrhizal colonization
The rate of mycorrhizal colonization was determined as described by Giovannetti and Mosse [53]. A 1 cm root segment was digested with a solution of 10% KOH at 90 °C for 20 min, acidified with 2% HCl for 5 min, stained with 0.05% triphenyl blue lactic acid glycerin solution (lactic acid/glycerin =1/1) at 90 °C for 30 min, and decolorized overnight with a solution of lactic acid glycerin (lactic acid/glycerin/water = 1/1/1 [v/v/v]). The root segments were observed under a microscope. The rate of infection of each root segment was assessed by the number of root mycorrhizal structures in each section and expressed as 0, 10, 20, ..., 100% of the root. The mycorrhizal colonization rate (%) was calculated as follows:

RNA extraction, cDNA library construction, and Illumina sequencing
Total RNA was isolated using a RNA Prep Pure Plant Kit (CWBIO, Beijing, China) according to the manufacturer's instructions. Total RNA was tested with an Agilent 2100 Bioanalyzer (Agilent Technologies, Santa Clara, CA, USA). The synthesis of cDNA was Mycorrhizal colonization rate = Σ 0 × root segment number + 10% × root segment number + 20% × root segment number + … ⋯ + 100% × root segment number ∕Total root segment number. performed using HiScript II 1st Strand cDNA Synthesis Kit (Vazyme, Nanjing, China). cDNA fragments that were preferentially 250 ~ 300 bp long were purified with an AMPure XP system (Beckman Coulter, Brea, CA, USA). The PCR products were purified again after PCR amplification, and the cDNA library was finally obtained [54]. And cDNA library was assessed on an Agilent Bioanalyzer 2100 system (Agilent Technologies). The libraries were sequenced on a HiSeq ® X Ten System (Illumina, San Diego, CA) by Novogene Co., Ltd. (Beijing, China).

Transcriptomic data analysis
To ensure the quality and reliability of the data analysis, it is necessary to filter the original data, including the removal of reads with an adapter, and remove the reads that contain N. N indicates that the nucleobase information cannot be determined. The low quality reads were then removed. The base number of qPHRED was ≤20, which comprised ≥50% of the whole read length. Moreover, the contents of Q20, Q30, and GC in the clean data were calculated. All follow-up analyses were based on the clean data high quality. Clean data obtained by filtering the raw data were aligned to the reference genome sequence of The program FeatureCounts (v. 1.5.0-p3) was used to calculate the readings that mapped to each gene [55]. The FPKM of each gene was calculated based on the length of gene, and the reading that mapped to the gene was calculated. DESeq2 software (1.20.0) was used to analyze the differential expression between the four treatments [56]. DEGs with |log2(Fold Change)| ≥ 1 and P-value < 0.05 were considered as differentially expressed genes (DEGs) after multiple correction for subsequent analyses. The clusterProfiler R package (3.4.4) was used for the Gene Ontology (GO) enrichment analysis of DEGs [57].
MapMan software (version 3.6.0RC1) (http:// mapman. gabipd. org/ web/ guest/ mapman) was used to generate functional assignments in the different pathways [58] for each input gene and the data visualization/interpretation of apple gene expression. Gene annotation in the pathway analysis was prepared via Mercator online software within the PlabiPD website (https:// www. plabi pd. de/ portal/ merca tor4) based on the DNA sequence and followed the default annotation parameter.

Measurement of root physiological parameters
The root physiological parameters included the activities of SOD, CAT, and POD, the contents of PRO, SUG, MDA, H 2 O 2 and O 2 · − . Each physiological parameter was measured using kits obtained from Suzhou Keming Biotechnology Co., Ltd. (Suzhou, China). All the measurements were performed three times, and the average was calculated for further analysis.

Gene cloning and function validation of MdWRKY40
MdWRKY40 (MD15G1039500) sequence information was obtained from the apple genome database (http:// www. rosac eae. org). Total RNA extraction and cDNA synthesis were conducted as described by RNA Extraction, cDNA library construction, and Illumina sequencing section. A fragment of 912 bp was obtained by PCR amplification, cloned into the pLB vector (TianGen, http:// www. tiang en. com/).
The CDS of MdWRKY40 was inserted into the PRI101-AN vector, which has a green fluorescent protein (GFP) tag. The constructed overexpression vector was transformed into Agrobacterium tumefaciens LBA4404. The positive A. tumefaciens was obtained by PCR and used to infect 'Orin' callus. The infected calli were cultured on MS solid media at 24 °C in the dark for 1-2 days. It was then transferred to a screening medium that contained 50 mg·L − 1 kanamycin and 250 mg·L − 1 carbenicillin. The overexpression of MdWRKY40 was confirmed by PCR.

Yeast one-hybrid test
The target gene fragments MdWRKY40, MdWRKY40-N (0-120 aa), MdWRKY40-C (121-303 aa) were ligated into the pGADT7 vector. The fragment of MdGLU promoter was cloned into the pHIS2 vector. A yeast one-hybrid test was conducted according to the manufacturer's instructions of Yeast transformation system 2 (TaKaRa, Dalian, China). The yeast one-hybrid strain was Y187 (Clontech, Takara Bio USA, San Jose, CA, USA). The yeast strain Y187 that contained the recombinant pHIS2 vectors was grown on -Trp/−His (−T/−H) screening media with different 3-AT concentrations to determine the optimal concentrations. To determine the interactions, the Y187 yeast strain that harbored the recombinant pGADT7 and pHIS2 plasmids was spotted onto media that lacked Trp, His, and Leu. The control was an empty pGADT7 plasmid. The primers used are listed in Supplemental Table S2.

Electrophoretic mobility shift assays
The sequence of MdWRKY40 was inserted into the pET-32a (+) expression vector (Novagen, Madison, WI, USA). The recombinant MdWRKY40 protein was expressed in E. coli BL21 (DE3), and the fusion protein MdWRKY40-His was purified by a His-Tagged Protein Purification Kit (CWBIO, Beijing, China). The biotinylated probe was synthesized by Sangon Biotech Co., Ltd. (Shanghai, China). The fusion protein, probe, and binding buffer were mixed in a centrifuge tube and incubated at 24 °C for 30 min. After 50% glycerol and 5 × loading buffer were added to the sample, non-denaturing acrylamide gel electrophoresis was performed, and the protein-nucleic acid strip was transferred to film placed on nylon. After the completion of UV crosslinking, the preheated Blocking Buffer closure was added, then HRP Conjugate and 20 mL new Blocking Buffer (ThermoFisher, Shanghai, China) were incubated at room temperature for 15 min. The Washing Buffer (ThermoFisher) was used after washing and developing.

LUC activity
MdWRKY40 full length CDS inserted into the pHBT-AvrRpm 1 carrier and promoter segments of MdGLU into the pFRK1-LUC-nos carrier. Both plasmids were converted simultaneously from the protoplasm of apple callus and then expressed for 6 h at 24 °C. Subsequently, the protoplasm was suspended in 100 μL of cell lysate. The 5 μL cell extract and 20 μL 1 mmol·L − 1 4-MUG were incubated at 37 °C at 1 h, and the 100 μL of 0.2 mol·L − 1 sodium acetate was added to the termination reaction. The LUC activity was determined using the Luciferase Reporting Analysis System (Promega, Madison, WI, USA).

Quantitative reverse transcription-PCR (qRT-PCR)
The cDNA was synthesized using a HiScript II 1st Strand cDNA Synthesis Kit (Vazyme, Nanjing, China). The reverse transcription reactions began with 500 ng of total RNA. The resulting first stand cDNA was diluted 10-fold with ddH 2 O, and then used as templates for qRT-PCR assays. The primers were designed for qRT-PCR by Primer 6.0 software (Premier Biosoft, Palo Alto, CA, USA). The internal reference gene was actin. The reaction system in the PCR of each primer was SYBR Green Mix 5 μL, primer (10 μM) 0.3 μL, cDNA 1 μL, and dd H 2 O 3.4 μL. The PCR procedures were 50 °C 2 min, 95 °C 10 min, 95 °C 15 s, 65 °C 60 s, 72 °C (30 cycles), and 72 °C 10 min. The primers were synthesized by Sangon Biotech Co., Ltd. The relative quantitative method used the 2 -∆∆CT method [59]. Each sample had three biological replicates. The primer sequences are shown in Supplementary Table S2.

Data analysis
The experimental data was expressed as the means and standard deviation (SD) of three biological replicates. The plant growth, mycorrhizal colonization rate and physiological data were analyzed by Duncan's test at the 0.05 level using SPSS v. 19.0 (IBM, Inc., Armonk, NY, USA). The qRT-PCR data were analyzed by t-test. An asterisk (*) indicates significant differences, where '*' represents significant differences at P < 0.05, and '**' represents highly significant differences at P < 0.01. The graphs were constructed using GraphPad Prism 8 (San Diego, CA, USA). The annotations of the DEGs were based on the databases of GO and MapMan software.